Canonical Allele Identifier: CA414983478
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790424T>G , CM000686.2:g.12790424T>G GRCh38
NC_000024.9:g.14902357T>G , CM000686.1:g.14902357T>G GRCh37
NC_000024.8:g.13411751T>G NCBI36
NG_008311.1:g.94198T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3579T>G ENSP00000498372.1:p.His1193Gln
ENST00000338981.7:c.3579T>G MANE Select ENSP00000342812.3:p.His1193Gln
ENST00000426564.6:n.3591T>G
NM_004654.3:c.3579T>G NP_004645.2:p.His1193Gln
XM_011531469.1:c.3579T>G XP_011529771.1:p.His1193Gln
XM_011531470.1:c.3345T>G XP_011529772.1:p.His1115Gln
XM_017030078.2:c.3594T>G XP_016885567.1:p.His1198Gln
NM_004654.4:c.3579T>G MANE Select NP_004645.2:p.His1193Gln